Active Ingredient: IBUPROFEN
Proprietary Name: MIDOL
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071002
Product Number: 001
Approval Date: Sep 2, 1987
Applicant Holder Full Name: BAYER HEALTHCARE LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information